A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569392



Internal ID16010115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49497216..49634103hg38UCSC Ensembl
Innerchr15:49789413..49926300hg19UCSC Ensembl
Innerchr15:47576705..47713592hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38136888
hg19136888
hg18136888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842971
Samples
Known GenesDTWD1, FAM227B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569392
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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